A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492559



Internal ID22550486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47482309..47488011hg38UCSC Ensembl
chr3:47523799..47529501hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg385703
hg195703
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836336
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492559
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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